Hollow TiO₂ nanoparticles (HNPs) capped with conducting polymers, such as polythiophene (PT), polypyrrole (PPy), and polyaniline (PANI), have been studied to be used as polarizability-tunable electrorheological (ER) fluids. The hollow shape of TiO₂ nanoparticles, achieved by the removal of the SiO₂ template, offers colloidal dispersion stability in silicone oil owing to the high number density. Conducting polymer shells, introduced on the nanoparticle surface using vapor deposition polymerization method, improve the yield stress of the corresponding ER fluids in the order of PANI < PPy < PT. PT-HNPs exhibited the highest yield stress of ca. 94.2 Pa, which is 5.0-, 1.5-, and 9.6-times higher than that of PANI-, PPy-, and bare HNPs, respectively. The improved ER response upon tuning with polymer shells is attributed to the space charge contribution arising from the movement of the charge carriers trapped by the heterogeneous interface. The ER response of studied ER fluids is consistent with the corresponding polarizability results as indicated by the permittivity and electrophoretic mobility measurements. In conclusion, the synergistic effect of hollow nanostructures and conducting polymer capping effectively enhanced the ER performance.

In this study, a flexible all-solid-state asymmetric supercapacitor (FASC) device has been successfully fabricated via full recycling of heated tobacco waste (HTW). Tobacco leaves and cellulose acetate tubes have been successfully carbonized (HTW-C) and mixed with metal oxides (MnO₂ and Fe₃O₄) to obtain highly active materials for supercapacitors. Moreover, poly(lactic acid) (PLA) filters have been successfully dissolved in an organic solvent and mixed with the as-prepared active materials using a simple paste mixing method. In addition, flexible MnO₂- and Fe₃O₄-mixed HTW-C/PLA electrodes (C-MnO₂/PLA and C-Fe₃O₄/PLA) have been successfully fabricated using the drop-casting method. The as-synthesized flexible C-MnO₂/PLA and C-Fe₃O₄/PLA electrodes have exhibited excellent electrical conductivity of 378 and 660 μS cm⁻¹, and high specific capacitance of 34.8 and 47.9 mF cm⁻² at 1 mA cm⁻², respectively. A practical FASC device (C-MnO₂/PLA//C-Fe₃O₄/PLA) has been assembled by employing the C-MnO₂/PLA as the positive electrode and C-Fe₃O₄/PLA as the negative electrode. The as-prepared FASC device showed a remarkable capacitance of 5.80 mF cm⁻² at 1 mA cm⁻². Additionally, the FASC device manifests stable electrochemical performance under harsh bending conditions, verifying the superb flexibility and sustainability of the device. To the best of our knowledge, this is the first study to report complete recycling of heated tobacco waste to prepare the practical FASC devices. With excellent electrochemical performance, the experiments described in this study successfully demonstrate the possibility of recycling new types of biomass in the future.

Thanks to the large number of pressurization-induced pores of appropriate size and the high bulk density, the pressurized physically activated carbon showed much higher effective ethanol uptake than chemically activated carbon.

Hard carbon derived from Eucalyptus green tree from Ethiopia was developed to enhance 1st cycle Coulombic efficiency as the anode for SIBs. The different heat treatment temperatures were applied for preparing hard carbon from Eucalyptus wood to form suitable disordered carbon structure, interlayer space, and effective pore. Hard carbon heat treated at 1400°C indicated the highest electrochemical properties such as discharge capacities and 1st cycle Coulombic efficiency. Especially, hard carbons heat treated above 1200°C indicated above 80% of 1st cycle Coulombic efficiency which are relatively high.

This study addresses the critical challenge of carbon corrosion in proton exchange membrane fuel cells (PEMFCs) by developing hybrid supports that combine the high surface area of carbon black (CB) with the superior crystallinity and graphitic structure of carbon nanofibers (CNFs). Two commercially available CB samples were physically activated and composited with two types of CNFs synthesized via chemical vapor deposition using different carbon sources. The structure, morphology, and crystallinity of the resulting CNF–CB hybrid supports were characterized, and the performances of these hybrid supports in mitigating carbon corrosion and enhancing the PEMFC performance was evaluated through full-cell testing in collaboration with a membrane electrode assembly (MEA) manufacturer (VinaTech, Seoul, Republic, of Korea), adhering to industry-standard fabrication and evaluation procedures. Accelerated stress tests following the US Department of Energy protocols revealed that incorporating CNFs enhanced the durability of the CB-based hybrid supports without compromising their performance. The improved performance of the MEAs with the hybrid carbon support is attributed to the ability of the CNF to act as a structural backbone, facilitate water removal, and provide abundant edge plane sites for anchoring the platinum catalyst, which promoted the oxygen reduction reaction and improved catalyst utilization. The findings of this study highlight the potential of CNF-reinforced CB supports for enhancing the durability and performance of PEMFCs.